Valorization of Chemical Wastes: Ir(biscarbene)-Catalyzed Transfer Hydrogenation of Inorganic Carbonates Using Glycerol

被引:24
作者
Cheong, Yeon-Joo [1 ]
Sung, Kihyuk [1 ]
Park, Sehoon [2 ]
Jung, Jaehoon [2 ]
Jang, Hye-Young [1 ]
机构
[1] Ajou Univ, Dept Energy Syst Res, Suwon 16499, South Korea
[2] Univ Ulsan, Dept Chem, Ulsan 44776, South Korea
基金
新加坡国家研究基金会;
关键词
Glycerol; Transfer hydrogenation; Carbonates; Iridium; Formate; Lactate; HETEROCYCLIC-CARBENE COMPLEXES; CATALYTIC CONVERSION; SELECTIVE CONVERSION; LACTIC-ACID; IRIDIUM; RHODIUM; CO2; BICARBONATE; GENERATION; REACTIVITY;
D O I
10.1021/acssuschemeng.0c00050
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Ir(biscarbene)-catalyzed transfer hydrogenation of sustainable and practical Cl sources (inorganic carbonates: K2CO3, KHCO3, Na2CO3, NaHCO3) with a green hydrogen source, glycerol, was conducted to afford formates and lactates with high turnover numbers (TONs) and turnover frequencies (TOFs) (formates (TON 16856 and TOF 843 h(-1)) and lactates (TON 32609 and TOF 1630 h(-1))). Jr catalysts possessing various biscarbene ligands were employed, and the structural effects of Ir(biscarbene) catalysts were reflected on the catalytic activity. The CO2 reduction activity of Ir(biscarbene) catalysts is strongly dependent on the structure of biscarbene ligand, i.e., the length of the alkyl chain between two carbene groups and the wing-tip substituent of carbenes, of which the detailed reaction mechanism composed of beta-hydride elimination of glycerol and CO2 reduction and different binding energies of CO2 with catalysts involving propylene- and methylene-linker-containing biscarbenes were elucidated by density functional theory calculations.
引用
收藏
页码:6972 / 6978
页数:7
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